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3-(Anthracen-9-yl)thiophene is a heterocyclic chemical compound with the molecular formula C18H26S. It features a thiophene ring fused with an anthracene moiety, both of which are aromatic hydrocarbons. 3-(anthracen-9-yl)thiophene is recognized for its high thermal stability, excellent charge transport properties, and strong fluorescence, making it a promising candidate for the development of organic electronic materials.

1689-08-3

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1689-08-3 Usage

Uses

Used in Organic Electronics Industry:
3-(Anthracen-9-yl)thiophene is utilized as a building block for the synthesis of organic semiconductors and optoelectronic devices due to its desirable electronic properties and molecular structure.
Used in Organic Photovoltaics:
In the field of organic photovoltaics, 3-(anthracen-9-yl)thiophene is employed for its potential to enhance the efficiency and performance of solar cells by improving charge transport and light absorption.
Used in Organic Light-Emitting Diodes (OLEDs):
3-(Anthracen-9-yl)thiophene serves as a key component in the development of OLEDs, where its strong fluorescence and electronic properties contribute to the creation of high-quality, energy-efficient light sources.
Used in Organic Field-Effect Transistors:
3-(anthracen-9-yl)thiophene is also used in the fabrication of organic field-effect transistors, where its charge transport characteristics are leveraged to improve the performance and stability of these transistors in various electronic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1689-08-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,8 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1689-08:
(6*1)+(5*6)+(4*8)+(3*9)+(2*0)+(1*8)=103
103 % 10 = 3
So 1689-08-3 is a valid CAS Registry Number.

1689-08-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-anthracen-9-ylthiophene

1.2 Other means of identification

Product number -
Other names 3-(anthracen-9-yl)thiophene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1689-08-3 SDS

1689-08-3Downstream Products

1689-08-3Relevant academic research and scientific papers

When Anthracene and Quinone Avoid Cycloaddition: Acid-Catalyzed Redox Neutral Functionalization of Anthracene to Aryl Ethers

Ding, Nan,Ding, Nan,Ding, Nan,Li, Zhi

, p. 4276 - 4282 (2020)

Benzoquinone and 9-phenylanthracene barely undergo anticipated cycloaddition under acid catalysis. Instead, 9-anthracenyl aryl ethers are obtained as unexpected products. Mechanistic studies indicate that the reaction likely undergoes an ionic mechanism between protonated anthracene species and nucleophilic oxygen of 1,4-benzoquinone or 1,4-hydroquinone. A variety of 9-anthracenyl aryl ethers are constructed with this method. Produced anthracenyl aryl ethers are potential scaffolds for new fluorescent molecules.

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